Lucio Nitsch
Università degli Studi di Napoli Federico II
H-index: 44
Europe-Italy
Top articles of Lucio Nitsch
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Genetics and molecular basis of congenital heart defects in Down syndrome: role of extracellular matrix regulation | Nunzia Mollo Roberta Scognamiglio Anna Conti Simona Paladino Lucio Nitsch | 2023/2/2 | |
Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression | Frontiers in Genetics | Laura De Rosa Dominga Fasano Lucrezia Zerillo Valeria Valente Antonella Izzo | 2022/5/13 |
Overexpression of the Hsa21 transcription factor RUNX1 modulates the extracellular matrix in trisomy 21 cells | Frontiers in Genetics | Nunzia Mollo Miriam Aurilia Roberta Scognamiglio Lucrezia Zerillo Rita Cicatiello | 2022/3/10 |
Human trisomic ipscs from down syndrome fibroblasts manifest mitochondrial alterations early during neuronal differentiation | Biology | Nunzia Mollo Matteo Esposito Miriam Aurilia Roberta Scognamiglio Rossella Accarino | 2021/6/30 |
Corrigendum: Pioglitazone Improves Mitochondrial Organization and Bioenergetics in Down Syndrome Cells | Frontiers in genetics | Nunzia Mollo Maria Nitti Lucrezia Zerillo Deriggio Faicchia Teresa Micillo | 2020/7/27 |
The centrosomal/basal body protein OFD1 is required for microtubule organization and cell cycle progression | Tissue and Cell | Mariaevelina Alfieri Daniela Iaconis Roberta Tammaro Lucia Perone Gaetano Calì | 2020/6/1 |
Targeting mitochondrial network architecture in Down syndrome and aging | Nunzia Mollo Rita Cicatiello Miriam Aurilia Roberta Scognamiglio Rita Genesio | 2020/4/29 | |
M170. GENETIC CHARACTERIZATION OF A COHORT OF PATIENTS AFFECTED BY SCHIZOPHRENIA. THE ROLE FOR RARE STRUCTURAL VARIANTS IN MODULATING TREATMENT RESISTANT ENDOPHENOTYPES … | Schizophrenia Bulletin | Annarita Barone Felice Iasevoli Marta Matrone Elisabetta Filomena Buonaguro Mariateresa Falco | 2020/4 |
P. 185 The role for rare structural variants in the genetics of treatment resistant schizophrenia: preliminary data | European Neuropsychopharmacology | A Barone M Falco F Iasevoli EF Buonaguro M Matrone | 2020/11/1 |
Clinical phenotype, immunological abnormalities, and genomic findings in patients with DiGeorge spectrum phenotype without 22q11. 2 deletion | The Journal of Allergy and Clinical Immunology: In Practice | Emilia Cirillo Maria Rosaria Prencipe Giuliana Giardino Roberta Romano Giulia Scalia | 2020/10/1 |
Co-Authors
